Canonical Allele Identifier: CA373724426
Gene: TMC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.72700537G>T , CM000671.2:g.72700537G>T GRCh38
NC_000009.11:g.75315453G>T , CM000671.1:g.75315453G>T GRCh37
NC_000009.10:g.74505273G>T NCBI36
NG_008213.1:g.183737G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297784.10:c.256G>T MANE Select ENSP00000297784.6:p.Glu86Ter
ENST00000644967.1:c.-77+5823G>T ENSP00000496159.1:n.-77+5823G>T
ENST00000645053.1:c.-77+5823G>T ENSP00000493838.1:n.-77+5823G>T
ENST00000645208.2:c.256G>T ENSP00000494684.1:p.Glu86Ter
ENST00000645773.1:c.236+5823G>T ENSP00000493698.1:n.236+5823G>T
ENST00000645787.1:n.296G>T
ENST00000646244.1:n.706G>T
ENST00000646619.1:c.-77+5823G>T ENSP00000493726.1:n.-77+5823G>T
ENST00000650689.1:n.660+5823G>T
ENST00000651183.1:c.-77+5823G>T ENSP00000498723.1:n.-77+5823G>T
ENST00000297784.9:c.256G>T ENSP00000297784.5:p.Glu86Ter
ENST00000340019.4:c.256G>T ENSP00000341433.3:p.Glu86Ter
NM_138691.2:c.256G>T NP_619636.2:p.Glu86Ter
XM_011518213.1:c.844G>T XP_011516515.1:p.Glu282Ter
XM_017014256.1:c.259G>T XP_016869745.1:p.Glu87Ter
NM_138691.3:c.256G>T MANE Select NP_619636.2:p.Glu86Ter